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. 2005 Aug 14;11(30):4618-22.
doi: 10.3748/wjg.v11.i30.4618.

Mutation of DNA polymerase beta in esophageal carcinoma of different regions

Affiliations

Mutation of DNA polymerase beta in esophageal carcinoma of different regions

Guo-Qiang Zhao et al. World J Gastroenterol. .

Abstract

Aim: To observe the variation of DNA polymerase beta (polbeta) in esophageal carcinoma.

Methods: Thirty specimens containing adjacent normal epithelial tissues were collected from patients in Linzhou region (a high risk area for esophageal squamous carcinoma) and 25 specimens were from a non-high risk area. Total RNA was extracted from the samples and reverse transcription polymerase chain reaction (RT-PCR) was performed. PCR products were cloned and sequenced to investigate the polbeta gene with DNASIS and OMIGA. Statistical significance was evaluated using the chi(2) test.

Results: High-incidence area group: polbeta gene variation was detected in 13 of 30 esophageal carcinoma tissue specimens, and only one variation was found in 30 corresponding adjacent normal tissue specimens. Non high-incidence area group: polbeta gene variation was detected in 5 of 25 esophageal carcinoma tissue specimens, and no variation was found in 25 corresponding adjacent normal tissue specimens. The incidence of polbeta gene variation observed in the high-incidence area group was significantly higher than in the non-high incidence area group. Two mutation hot spots (454-466 and 648-670 nt) and a 58 bp deletion (177-234 nt) were found.

Conclusion: Variations of polbeta perform different functions between the high-incidence areas and the other areas, and may play a more important role in the high-incidence areas.

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Figures

Figure 1
Figure 1
RT-PCR amplification of polβ gene. Lanes 1, 2 and 7: Normal size of PCR products of H1, H2 and H3; lanes 3-6: shorter size of PCR product of H5, H8, H10, and H16; M: DNA marker (from top to bottom: 1 000, 900, 800, 700, 600, 500, 400, 300, 200, 100 bp).
Figure 2
Figure 2
Mutations in the polβ gene. A: 660 nt A→G mutation in H4 carcinoma; B: 670 nt A→G mutation in N1 carcinoma; C: 613 nt A→T mutation in H28 carcinoma.
Figure 3
Figure 3
Comparison between wild type polβ gene fragment and six gene fragments with deletion (177→234 nt).

References

    1. Okuda E, Osugi H, Morimura K, Takada N, Takemura M, Fukushima S, Higashino M, Kinoshita H. Detection of p53 gene mutations in human esophageal squamous cell carcinomas using a p53 yeast functional assay: possible difference in esophageal carcinogenesis between the young and the elderly group. Clin Cancer Res. 2001;7:600–606. - PubMed
    1. Nie Y, Yang G, Song Y, Zhao X, So C, Liao J, Wang LD, Yang CS. DNA hypermethylation is a mechanism for loss of expression of the HLA class I genes in human esophageal squamous cell carcinomas. Carcinogenesis. 2001;22:1615–1623. - PubMed
    1. Kokoska RJ, Bebenek K, Boudsocq F, Woodgate R, Kunkel TA. Low fidelity DNA synthesis by a y family DNA polymerase due to misalignment in the active site. J Biol Chem. 2002;277:19633–19638. - PubMed
    1. Ito T, Shimada Y, Hashimoto Y, Kaganoi J, Kan T, Watanabe G, Murakami Y, Imamura M. Involvement of TSLC1 in progression of esophageal squamous cell carcinoma. Cancer Res. 2003;63:6320–6326. - PubMed
    1. Kuroki T, Trapasso F, Yendamuri S, Matsuyama A, Alder H, Mori M, Croce CM. Allele loss and promoter hypermethylation of VHL, RAR-beta, RASSF1A, and FHIT tumor suppressor genes on chromosome 3p in esophageal squamous cell carcinoma. Cancer Res. 2003;63:3724–3728. - PubMed

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